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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1433680생성일: 2026년 10월 26일

Water → N-Methyl-4-benzyloxy-2-fluoroaniline

https://huagongshe.com/reaction/1433680

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium borohydrideHCID 4311764—
반응물Tetrahydrofuran ethyl acetateHCID 21939870—
반응물N-{1-(1H-Benzotriazolyl)methyl}-4-benzyloxy-2-fluoroanilineHCID 22936313—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
생성물N-Methyl-4-benzyloxy-2-fluoroanilineHCID 2293665864.9%

반응 단계

After dissolving N-{1-(1H-benzotriazolyl)methyl}-4-benzyloxy-2-fluoroaniline (14.13 g, 40.56 mmol) in N,N-dimethylformamide (200 ml), methanol (150 ml) and ethanol (50 ml), there was added sodium borohydride (3.06 g, 81.12 mmol) and the mixture was stirred for 2.5 hours at room temperature. There was further added sodium borohydride (0.78 g, 20.28 mmol), and the mixture was stirred for 13.5 hours at room temperature. Water was added to the reaction solution, extraction was performed with ethyl acetate-tetrahydrofuran, the extract was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was adsorbed onto silica gel and purified by silica gel column chromatography (hexane-ethyl acetate system) to obtain the title compound (5.98 g, 26.31 mmol, 64.87%) as light yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07612092B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-23425df8c8ec4f1f93c19d4789828845
출처 메모uspto-grants-2009_11